Nayak D P, Davis A R
J Virol. 1976 Mar;17(3):745-55. doi: 10.1128/JVI.17.3.745-755.1976.
The nature of the endogenous viral DNA sequences in guinea pig cells was studied by hybridization. A segment of the viral RNA (r-VRNA) hybridizing to abundant (or reiterated) DNA sequences (R-VDNA) was isolated by recycling to a Cot of 300. The hybridization of the recycled VRNA, as well as the total VRNA, was followed by determining their kinetics and by Wetmur-Davidson analysis. The kinetics of hybridization of total VRNA were complex, did not follow a second-order kinetics, and revealed two slopes by Wetmur-Davidson analysis. The recycled RNA, on the other hand, had a second-order reaction rate expected of the hybridization between a single species of RNA and DNA sequences and yielded a single straight line in a Wetmur-Davidson plot. The Cot1/2 and slope of the recycled r-VRNA was almost identical to that of the abundant VDNA sequences obtained from the hybridization data of the total VRNA. Guinea pig 28S rRNA with or without recycling was used in monitoring hybridization rate. The kinetics of hybridization of 28S RNA followed a second-order reaction and produced a single straight line by Wetmur-Davidson plot, with a second-order reassociation rate constant of 9.6 x 10(-3) liters/mol-s, a Cot1/2 of 104 mol-s/liter, and reiteration frequency of 146. There was no difference in the kinetics of hybridization of 28S RNA before and after recycling. These experiments showed that guinea pig cells contain two classes of VDNA sequences. (i) R-VDNA sequences with a second-order reassociation rate constant of 8.2 x 10(-4) liters/mol-s, a Cot1/2 of 1,219 mol-s/liter, and a reiteration frequency of 12 represent 37.5% of the viral genome. (ii) Unique VDNA sequences with a second-order reassociation rate constant of 1.2 x 10(-4) liters/mol-s, a Cot1/2 of 7,692 mol-s/liter, and a reiteration frequency of 2 represent 62.5% of the viral genome.
通过杂交研究了豚鼠细胞内源性病毒DNA序列的性质。通过循环至Cot值为300,分离出一段与丰富(或重复)DNA序列(R-VDNA)杂交的病毒RNA片段(r-VRNA)。回收的VRNA以及总VRNA的杂交,通过测定其动力学和进行Wetmur-Davidson分析来跟踪。总VRNA的杂交动力学很复杂,不遵循二级动力学,并且通过Wetmur-Davidson分析显示出两个斜率。另一方面,回收的RNA具有单一种类的RNA与DNA序列杂交预期的二级反应速率,并且在Wetmur-Davidson图中产生一条直线。回收的r-VRNA的Cot1/2和斜率与从总VRNA的杂交数据获得的丰富VDNA序列的几乎相同。有或没有回收的豚鼠28S rRNA用于监测杂交速率。28S RNA的杂交动力学遵循二级反应,并且通过Wetmur-Davidson图产生一条直线,二级重结合速率常数为9.6×10(-3)升/摩尔·秒,Cot1/2为104摩尔·秒/升,重复频率为146。回收前后28S RNA的杂交动力学没有差异。这些实验表明豚鼠细胞含有两类VDNA序列。(i)二级重结合速率常数为8.2×10(-4)升/摩尔·秒,Cot1/2为1219摩尔·秒/升,重复频率为12的R-VDNA序列占病毒基因组的37.5%。(ii)二级重结合速率常数为1.2×10(-4)升/摩尔·秒,Cot1/2为7692摩尔·秒/升,重复频率为2的独特VDNA序列占病毒基因组的62.5%。